Chronic Eosinophilic Leukemia Presenting as Cardiac Failure.

IF 0.7 Q4 HEMATOLOGY
Nii Boi-Doku Pepra-Ameyaw, William Kwasi Ghunney, Eugene Baafi Ampofo, Edeghonghon Olayemi
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引用次数: 0

Abstract

Chronic eosinophilic leukemia (CEL) is a rare chronic myeloproliferative disorder characterized by sustained eosinophilia. Although the incidence of CEL is uncertain, it can be clinically devastating as it has a propensity to affect several important organ systems. This is of particular significance in Sub-Saharan Africa where helminthic infections are a more prevalent cause of eosinophilia. To the best of our knowledge, we present the first reported case of CEL complicated by cardiac disease in a Ghanaian. He presented with a history of orthopnoea and dyspnoea on exertion, and examination revealed a pansystolic murmur over the mitral region and moderate splenomegaly. Good symptomatic control was achieved using hydroxyurea after which haematologic and cytogenetic remission was achieved after 12 weeks on a tyrosine kinase inhibitor. Physicians working in low resource environments should exclude clonality in patients presenting with eosinophilia and end-organ damage.

Abstract Image

Abstract Image

Abstract Image

慢性嗜酸性粒细胞白血病表现为心力衰竭。
慢性嗜酸性粒细胞白血病(CEL)是一种罕见的慢性骨髓增生性疾病,以持续嗜酸性粒细胞增多为特征。虽然CEL的发病率尚不确定,但它可能是临床上毁灭性的,因为它有影响几个重要器官系统的倾向。这在撒哈拉以南非洲尤其重要,因为蠕虫感染是嗜酸性粒细胞增多症更普遍的原因。据我们所知,我们提出了第一例报告的CEL合并心脏病在加纳人。他有直立呼吸和用力时呼吸困难的病史,检查发现二尖瓣区有全收缩期杂音和中度脾肿大。使用羟基脲获得了良好的症状控制,在使用酪氨酸激酶抑制剂12周后,血液学和细胞遗传学得到缓解。在低资源环境中工作的医生应排除出现嗜酸性粒细胞增多和终末器官损伤的患者的克隆性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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审稿时长
13 weeks
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